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dc.creatorUS National Cancer Instituteen_GB
dc.date.accessioned2005-08-23T12:05:46Z
dc.date.available2005-08-23T12:05:46Z
dc.date.created2003-02-01en_GB
dc.date.issued2005-08-23T12:05:46Z
dc.identifierNSC59611en_GB
dc.identifier.urihttp://www.dspace.cam.ac.uk/handle/1810/56324
dc.format.extent7749 bytes
dc.format.extent7051 bytes
dc.format.mimetypechemical/x-cml
dc.format.mimetypechemical/x-cml
dc.language.isoen_GB
dc.publisherUnilever Center for Molecular Informatics, Cambridge Universityen_GB
dc.titleNSC59611en_GB
dc.title.alternativeD-Homo-17a-oxaandrost-4-ene-3,17-dione deriv. of 2H-Phenanthro[2, 1-b]pyranen_GB
dc.title.alternativeTestololactone, 7.alpha.-hydroxy-en_GB
dc.title.alternative13, 17-Secoandrost-4-en-17-oic acid, 7.alpha., 13.alpha.-dihydroxy-3-oxo-, .delta.-lactoneen_GB
dc.title.alternative17a-Oxa-D-homoandrost-4-ene-3,17-dione, 7.alpha.-hydroxy-en_GB
dc.title.alternative7.alpha.-Hydroxytestololactoneen_GB
dc.title.alternative7-.alpha.-hydroxy-D-homo-17a-oxa-androst-4-ene-3,17-dione (9CI)en_GB
dc.title.alternative7-.alpha.-hydroxytestololactoneen_GB
dc.typeChemical Structuresen_GB
dc.identifier.inchikeyFOXXEHXXDDNIKJ-GBHAUCNQSA-N
dc.identifier.inchiInChI=1S/C19H26O4/c1-18-7-5-12(20)9-11(18)10-15(21)17-13(18)6-8-19(2)14(17)3-4-16(22)23-19/h9,13-15,17,21H,3-8,10H2,1-2H3/t13-,14-,15+,17+,18-,19-/m0/s1
dc.identifier.ichiC19H26O4,1H3-18-8H2-5H2-12(20)3H-11(18)10H2-16H(22H)17H-14H(18)7H2-9H2-19(2H3)15H(17)6H2-4H2-13(21)23-19en_GB


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  • WWMM
    The WorldWideMolecularMatrix, an Open collection of information on small molecules

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